Sulfamethoxazole

CAS Number 723-46-6
Molecular Formula C10H11N3O3S
Molecular Weight 253.276 g/mol
InChI Key JLKIGFTWXXRPMT-UHFFFAOYSA-N
LogP 0.9
Synonyms
  • Sulfamethoxazole
  • Sulphamethoxazole
  • Sulfisomezole
  • Gantanol
  • Sulfamethoxazol
  • Metoxal
  • Sulfamethylisoxazole
  • Simsinomin
  • Radonil
  • Sinomin
  • Sulphamethoxazol
  • Sulpha-methoxizole
  • Sulfamethalazole
  • Azo-gantanol
  • 4-Amino-N-(5-methyl-3-isoxazolyl)benzenesulfonamide
  • Sulphamethylisoxazole
  • Urobak
  • Sulfamethoxizole
  • 3-Sulfanilamido-5-methylisoxazole
  • Gantanol-DS
  • 4-amino-N-(5-methylisoxazol-3-yl)benzenesulfonamide
  • Bactrimel
  • Gamazole
  • Azo gantanol
  • Sulfametoxazol
  • Sulphisomezole
  • Solfametossazolo
  • Sulfamethoxazolum
  • 5-Methyl-3-sulfanilamidoisoxazole
  • Ro 4-2130
  • MS 53
  • 3-Sulphanilamido-5-methylisoxazole
  • Benzenesulfonamide, 4-amino-N-(5-methyl-3-isoxazolyl)-
  • 5-Methyl-3-sulphanil-amidoisoxazole
  • 3-(p-Aminophenylsulfonamido)-5-methylisoxazole
  • 5-Methyl-3-sulfanylamidoisoxazole
  • N'-(5-Methyl-3-isoxazolyl)sulfanilamide
  • N1-(5-Methyl-3-isoxazolyl)sulfanilamide
  • N'-(5-Methylisoxazol-3-yl)sulphanilamide

Applications:


Separation of Antibiotics in Mixed-mode chromatography

 

A complex mixture of sulphonamide, macrolide, tetracycline and fluoroquinolone antibiotics were separated in one run using mixed-mode chromatography with LC/MS -compatible conditions. All compounds are separated based on reversed-phase and/or ion-exchange mechanism. Method can be used for analysis of various classes of antibiotics and related impurities in different sample matrices (blood, urine, soil, waste water).



Application Analytes:

Carboxymethylcysteine
Chlortetracycline
Dapsone
Flumequine
Josamycin
Marbofloxacin
Norfloxacin
Oxytetracycline
Spiramycin
Sulfamethoxazole
Sulfonamides
Sulphadiazine
Sulphaguanidine
Sulphanilamide
Sulphaquinoxaline
Tetracycline
Tylosin